STP and Tip are essential for herpesvirus saimiri oncogenicity

J Virol. 1998 Feb;72(2):1308-13. doi: 10.1128/JVI.72.2.1308-1313.1998.

Abstract

Mutant forms of herpesvirus saimiri (HVS) subgroup C strain 488 with deletions in either STP-C488 or Tip were constructed. The transforming potentials of the HVS mutants were tested in cell culture and in common marmosets. Parental HVS subgroup C strain 488 immortalized common marmoset T lymphocytes in vitro to interleukin-2-independent growth, but neither of the deletion mutants produced such growth transformation. Wild-type HVS produced fatal lymphoma within 19 to 20 days of experimental infection of common marmosets, while HVS deltaSTP-C488 and HVS deltaTip were nononcogenic. Virus was repeatedly isolated from the peripheral blood of marmosets infected with mutant virus for more than 5 months. These results demonstrate that STP-C488 and Tip are not required for replication or persistence, but each is essential for transformation in cell culture and for lymphoma induction in common marmosets.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Gene Deletion*
  • Genes, Viral*
  • Herpesviridae Infections / virology*
  • Herpesvirus 2, Saimiriine / genetics*
  • Herpesvirus 2, Saimiriine / pathogenicity
  • Oncogene Proteins, Viral / genetics*
  • Phosphoproteins / genetics*
  • T-Lymphocytes / virology*
  • Tumor Virus Infections / virology*
  • Viral Proteins / genetics*
  • Virulence / genetics

Substances

  • Oncogene Proteins, Viral
  • Phosphoproteins
  • STP-C488 protein, Herpesvirus saimiri
  • Viral Proteins
  • tyrosine kinase interacting protein, Saimiriine herpesvirus 2